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Scope of the Agreement Contract Clauses (18)
Grouped Into 2 Collections of Similar Clauses From Business Contracts
This page contains Scope of the Agreement clauses in business contracts and legal agreements. We have organized these clauses into groups of similarly worded clauses.
Scope of the Agreement. 2.1. Generally. Each Party shall: (a) contribute to the Study such resources as are necessary to fulfill its obligations set forth in this Agreement; and (b) act in good faith in performing its obligations under this Agreement and each Related Agreement to which it is a Party. 2.2. Manufacturing Delay. Each Party shall notify the other Party as promptly as possible in the event of any Manufacturing delay that is likely to adversely affect supply of its Compound as contemplated by this Agreement.... 2.3. Compound Commitments. 2.3.1 Company agrees to Manufacture and supply the Company Compound for purposes of the Study in accordance with Article 8, and Company hereby represents and warrants to Merck that, at the time of Delivery of the Company Compound, such Company Compound shall have been Manufactured and supplied in compliance with: (a) the Specifications for the Company Compound; (b) the Clinical Quality Agreement; and (c) all Applicable Law, including cGMP and health, safety and environmental protections. 2.3.2 Merck agrees to Manufacture and supply the Merck Compound for purposes of the Study in accordance with Article 8, and Merck hereby represents and warrants to Company that, at the time of Delivery of the Merck Compound, such Merck Compound shall have been Manufactured and supplied in compliance with: (a) the Specifications for the Merck Compound; (b) the Clinical Quality Agreement; and (c) all Applicable Law, including cGMP and health, safety and environmental protections. 8 CONFIDENTIAL 2.3.3 Without limiting the foregoing, each Party is responsible for obtaining all regulatory approvals (including facility licenses) that are required to Manufacture its Compound in accordance with Applicable Law (provided that, for clarity, Company shall be responsible for obtaining Regulatory Approvals for the Study as set forth in Section 3.4). 2.4. Delegation of Obligations. Each Party shall have the right to delegate any portion of its obligations hereunder as follows: (a) to such Party's Affiliates; (b) to Third Parties that are set forth in the Protocol as performing Study activities or as conducting Sample Testing for such Party; (c) to the extent related to the Manufacture of such Party's Compound; and (d) upon the other Party's prior written consent. Any and all Third Parties to whom a Party delegates any of its obligations hereunder are referred to as "Subcontractors". Notwithstanding any delegation of its obligations hereunder, each Party shall remain solely and fully liable for the performance of its Affiliates and Subcontractors to which such Party delegates the performance of its obligations under this Agreement. Each Party shall ensure that each of its Affiliates and Subcontractors performs such Party's obligations pursuant to the terms of this Agreement, including the Appendices and Schedules attached hereto. Each Party shall use reasonable efforts to obtain and maintain copies of documents relating to the obligations performed by such Affiliates and Subcontractors that are required to be provided to the other Party under this Agreement. 2.5. Compounds. This Agreement does not create any obligation on the part of Merck to provide the Merck Compound for any activities other than the Study, nor does it create any obligation on the part of Company to provide the Company Compound for any activities other than the Study.
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ONCOSEC MEDICAL Inc contract
Scope of the Agreement. 2.1. 2.1 Generally. Each Party shall: (a) contribute to the Study such resources as are necessary to fulfill its obligations set forth in this Agreement; and (b) act in good faith in performing its obligations under this Agreement and each Related Agreement to which it is a Party. 2.2. 2.2 Manufacturing Delay. Each Party shall notify the other Party as promptly as possible in the event of any Manufacturing delay that is likely to adversely affect supply of its Compound Compound(s) as contemplate...d by this Agreement. 2.3. 2.3 Compound Commitments. 2.3.1 Company agrees to Manufacture and supply the Company Compound Compounds for purposes of the Study in accordance with Article 8, and Company hereby represents and warrants to Merck MSD that, at the time of Delivery of the Company Compounds, such Company Compounds shall have been Manufactured and supplied in compliance with: (a) the Specifications for the Company Compounds; (b) the Clinical Quality Agreement; and (c) all Applicable Law, including cGMP and health, safety and environmental protections. 2.3.2 MSD and/or its Affiliate(s) agrees to Manufacture and supply the MSD Compound for purposes of the Study in accordance with Article 8, and MSD and/or its Affiliate(s) hereby represents and warrants to Company that, at the time of Delivery of the MSD Compound, such Company MSD Compound shall have been Manufactured and supplied in compliance with: (a) the Specifications for the Company MSD Compound; (b) the Clinical Quality Agreement; and (c) all Applicable Law, including cGMP and health, safety and environmental protections. 2.3.2 Merck agrees to Manufacture and supply the Merck Compound for purposes of the Study in accordance with Article 8, and Merck hereby represents and warrants to Company that, at the time of Delivery of the Merck Compound, such Merck Compound shall have been Manufactured and supplied in compliance with: (a) the Specifications for the Merck Compound; (b) the Clinical Quality Agreement; and (c) all Applicable Law, including cGMP and health, safety and environmental protections. 8 CONFIDENTIAL 9 Confidential 2.3.3 Without limiting the foregoing, each Party is responsible for obtaining all regulatory approvals (including facility licenses) that are required to Manufacture its Compound Compound(s) in accordance with Applicable Law (provided that, for clarity, Company shall be responsible for obtaining Regulatory Approvals for the Study as set forth in Section 3.4). 2.4. 2.4 Delegation of Obligations. Each Party shall have the right to delegate any portion of its obligations hereunder as follows: (a) to such Party's Affiliates; (b) to Third Parties that are set forth on Schedule 2.4 or are set forth in the Protocol as performing Study activities or as conducting Sample Testing for such Party; (c) to the extent related to Third Parties solely in connection with the Manufacture of such Party's Compound; Compound(s); and (d) upon the other Party's prior written consent. Any and all Third Parties to whom a Party delegates any of its obligations hereunder are referred to as "Subcontractors". Notwithstanding any delegation of its obligations hereunder, each Party shall remain solely and fully liable for the performance of its Affiliates and Subcontractors to which such Party delegates the performance of its obligations under this Agreement. Each Party shall ensure that each of its Affiliates and Subcontractors performs such Party's obligations pursuant to the terms of this Agreement, including the Appendices and Schedules attached hereto. Each Party shall use reasonable efforts to obtain and maintain copies of documents relating to the obligations performed by such Affiliates and Subcontractors that are required to be provided to the other Party under this Agreement. 2.5. 2.5 Compounds. This Agreement does not create any obligation on the part of Merck MSD and/or its Affiliate(s) to provide the Merck MSD Compound for any activities other than the Study, nor does it create any obligation on the part of Company to provide the Company Compound Compounds for any activities other than the Study.
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IO Biotech, Inc. contract
Scope of the Agreement. 2.1. Generally. 2.1 Each Party shall: (a) shall contribute to the Study such resources as are reasonably necessary to fulfill its obligations set forth in this Agreement; and (b) Agreement. 2.2 Each Party agrees to act in good faith in performing its obligations under this Agreement and each Related Agreement to which it is a Party. 2.2. Manufacturing Delay. Each Party Agreement, and shall notify the other Party as promptly as possible in the event of any Manufacturing delay that is likely to ad...versely affect supply of its Compound as contemplated by this Agreement. 2.3. Compound Commitments. 2.3.1 Company agrees to Manufacture and supply the Company Compound for purposes of the Study in accordance with Article 8, and Company hereby represents and warrants to Merck that, at the time of Delivery of the Company Compound, such Company Compound shall have been Manufactured and supplied in compliance with: (a) the Specifications for the Company Compound; (b) the Clinical Quality Agreement; and (c) all Applicable Law, including cGMP and health, safety and environmental protections. 2.3.2 Merck agrees to Manufacture and supply the Merck Compound for purposes of the Study in accordance with Article 8, and Merck hereby represents and warrants to Company that, at the time of Delivery of the Merck Compound, such Merck Compound shall have been Manufactured and supplied in compliance with: (a) the Specifications for the Merck Compound; (b) the Clinical Quality Agreement; and (c) all Applicable Law, including cGMP and health, safety and environmental protections. 8 CONFIDENTIAL 2.3.3 Without limiting the foregoing, each Party is responsible for obtaining all regulatory approvals (including facility licenses) that are required to Manufacture its Compound in accordance with Applicable Law (provided that, for clarity, Company shall be responsible for obtaining Regulatory Approvals for the Study as set forth in Section 3.4). 2.4. Delegation of Obligations. 2.3 Each Party shall have the right to delegate subcontract any portion of its obligations hereunder as follows: (a) to such Party's Affiliates; (b) to Third Parties that are set forth in the Protocol as performing Study activities or as conducting Sample Testing for such Party; (c) to the extent related to the Manufacture of such Party's Compound; and (d) upon the other Party's prior written consent. Any and all Third Parties to whom a Party delegates any of its obligations hereunder are referred to as "Subcontractors". Notwithstanding any delegation of its obligations hereunder, each subcontractors ("Subcontractors"). Each Party shall remain solely and fully liable for the performance of its Affiliates and Subcontractors to which such Party delegates the performance of its obligations under this Agreement. Subcontractors. Each Party shall ensure that each of its Affiliates and Subcontractors subcontractors performs such Party's its obligations pursuant to the terms of this Agreement, including the Appendices and Schedules attached hereto. For clarity, to the extent that a Party has an obligation under this Agreement to perform an action or to meet a standard, and such Party subcontracts such obligation, such Party shall be responsible for any failure by such Party's Subcontractor to perform the action or meet the standard. Each Party shall use reasonable efforts to obtain and maintain copies of documents relating to the obligations performed by such Affiliates Subcontractors that are held by or under the control of such Subcontractors and Subcontractors that are required to be provided to the other Party under this Agreement. 2.5. Compounds. 2.4 This Agreement does not create any obligation on the part of Merck to provide the Merck Compound for any activities other than the Study, nor does it create any obligation on the part of Company Vaccinex to provide the Company Vaccinex Compound for any activities other than the Study. [***] INDICATES MATERIAL THAT WAS OMITTED AND FOR WHICH CONFIDENTIAL TREATMENT WAS REQUESTED. ALL SUCH OMMITTED MATERIAL WAS FILED SEPARATELY WITH THE SECURITIES AND EXCHANGE COMMISSION PURSUANT TO RULE 406 PROMULGATED UNDER THE SECURITIES ACT OF 1933, AS AMENDED. Note: Reference to "Merck" in this document refers to the Group of Companies affiliated with Merck KGaA, Darmstadt, Germany. 9 2.5 Subject to Section 3.10 below, nothing in this Agreement shall (i) prohibit either Party from performing clinical studies other than the Study relating to its own Compound, either individually or in combination with any other compound or product, in any therapeutic area, or (ii) create an exclusive relationship between the Parties with respect to any Compound.
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VACCINEX, INC. contract
Scope of the Agreement. 2.1. Generally. *** INDICATES MATERIAL THAT WAS OMITTED AND FOR WHICH CONFIDENTIAL TREATMENT WAS REQUESTED. ALL SUCH OMITTED MATERIAL WAS FILED SEPARATELY WITH THE SECURITIES AND EXCHANGE COMMISSION PURSUANT TO RULE 406 PROMULGATED UNDER THE SECURITIES ACT OF 1933, AS AMENDED. 7 2.1 Each Party shall: (a) shall contribute to the Study such resources as are necessary to fulfill its obligations set forth in this Agreement; and (b) Agreement. 2.2 Each Party agrees to act in good faith in performing ...its obligations under this Agreement and each Related Agreement to which it is a Party. 2.2. Manufacturing Delay. Each Party Agreement, and shall notify the other Party as promptly as possible in the event of any Manufacturing delay that is likely to adversely affect supply of its Compound as contemplated by this Agreement. 2.3. Compound Commitments. 2.3.1 Company Representations and Warranties. 2.3.1. Syndax agrees to Manufacture and supply the Company Syndax Compound for purposes of the Study as set forth in accordance with Article 8, and Company Syndax hereby represents and warrants to Merck the Alliance that, at the time of Delivery of the Company Syndax Compound, such Company Syndax Compound shall have been Manufactured and supplied in compliance with: (i) the Specifications for the Syndax Compound; (ii) the Clinical Quality Agreements; and (iii) all Applicable Law, including cGMP and health, safety and environmental protections. The Alliance agrees to Manufacture and supply the Alliance Compound for purposes of the Study as set forth in Article 8, and the Alliance hereby represents and warrants to Syndax that, at the time of Delivery of the Alliance Compound, such Alliance Compound shall have been Manufactured and supplied in compliance with: (a) the Specifications for the Company Alliance Compound; (b) the Clinical Quality Agreement; Agreements; and (c) all Applicable Law, including cGMP and health, safety and environmental protections. 2.3.2 Merck agrees to Manufacture and supply the Merck Compound for purposes of the Study in accordance with Article 8, and Merck hereby represents and warrants to Company that, at the time of Delivery of the Merck Compound, such Merck Compound shall have been Manufactured and supplied in compliance with: (a) the Specifications for the Merck Compound; (b) the Clinical Quality Agreement; and (c) all Applicable Law, including cGMP and health, safety and environmental protections. 8 CONFIDENTIAL 2.3.3 Without limiting the foregoing, each Party is responsible for obtaining all regulatory approvals (including facility licenses) that are required to Manufacture its Compound in accordance with Applicable Law (provided that, that for clarity, Company Syndax shall be responsible for obtaining Regulatory Approvals for the Study as set forth in Section 3.4). 3.3). 2.4. Delegation of Obligations. Each Party shall have the right to delegate subcontract any portion of its obligations hereunder as follows: (a) to such Party's Affiliates; (b) to Third Parties that are set forth in the Protocol as performing Study activities or as conducting Sample Testing for such Party; (c) to the extent related to the Manufacture of such Party's Compound; and (d) upon the other Party's prior written consent. Any and all Third Parties to whom a Party delegates any of its obligations hereunder are referred to as "Subcontractors". Notwithstanding any delegation of its obligations hereunder, each subcontractors ("Subcontractors"). Each Party shall remain solely and fully liable for the performance of its Affiliates and Subcontractors to which such Party delegates the performance of its obligations under this Agreement. Subcontractors. Each Party shall ensure that each of its Affiliates and Subcontractors subcontractors performs such Party's its obligations pursuant to the terms of this Agreement, including the Appendices and Schedules attached hereto. For clarity, to the extent that a Party has an obligation under this Agreement to perform an action or to meet a standard, and such Party subcontracts such obligation, such Party shall be responsible for any failure by such Party's Subcontractor to perform the action or meet the standard. Each Party shall use reasonable efforts to obtain and maintain copies of documents relating to the obligations performed by such Affiliates Subcontractors that are held by or under the control of such Subcontractors and Subcontractors that are required to be provided to the other Party under this Agreement. 2.5. Compounds. *** INDICATES MATERIAL THAT WAS OMITTED AND FOR WHICH CONFIDENTIAL TREATMENT WAS REQUESTED. ALL SUCH OMITTED MATERIAL WAS FILED SEPARATELY WITH THE SECURITIES AND EXCHANGE COMMISSION PURSUANT TO RULE 406 PROMULGATED UNDER THE SECURITIES ACT OF 1933, AS AMENDED. 8 2.5 This Agreement does not create any obligation on the part of Merck the Alliance to provide the Merck Alliance Compound for any activities other than the Study, nor does it create any obligation on the part of Company Syndax to provide the Company Syndax Compound for any activities other than the Study. 2.6 Subject to Section 3.10 below, nothing in this Agreement shall (i) prohibit either Party from performing clinical studies other than the Study relating to its own Compound, either individually or in combination with any other compound or product, in any therapeutic area, or (ii) create an exclusive relationship between the Parties with respect to any Compound.
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Syndax Pharmaceuticals Inc contract
Scope of the Agreement. Subject to the terms and conditions of this Agreement, Lazuriton Nano Biotech hereby appoints Distributor as an authorized distributor of the Nano fertilizers products manufactured by Lazuriton Nano Biotech listed in Exhibit A (the "Products") in the territory set forth on Exhibit A (the "Territory"), and Distributor accepts such appointment. Distributor may not sell the Products to customers in another territory where Lazuriton Nano Biotech has reserved such territory exclusively for itself or ...another distributor. Distributor not, directly or indirectly (including through its affiliates), actively solicit orders for any of the Products in any such territory; provided, however, Distributor shall not be prevented from accepting and filling unsolicited orders for the Products from a customer located outside the Territory. (b) Products. Lazuriton Nano Biotech reserves the right to discontinue or modify the Products, modify the Product specifications, or replace the Products with other Nano fertilizers products, in its sole discretion; provided, however, except as required by law, any such discontinuations, modifications, or replacements will not apply to Products that are subject to an outstanding purchase order accepted by Lazuriton Nano Biotech. (c) Competitive Products. During the Term (as defined below), Distributor shall not promote or sell, directly or indirectly, any product manufactured or offered for sale by another person or entity, which product competes with the Products (each, a "Competing Product"). Distributor warrants that it does not promote or sell, directly or indirectly, any Competing Product as of the Effective Date. During the Term, Distributor shall disclose to Lazuriton Nano Biotech any new Nano fertilizers products that Distributor intends to promote or sell, as well as the manufacturer of such products, prior to promoting or selling such products, and Lazuriton Nano Biotech shall determine, in its sole discretion, whether such products are Competing Products. (d) Independent Contractors. The relationship of Lazuriton Nano Biotech and Distributor established by this Agreement is that of independent contractors and nothing contained herein shall be construed to (i) give either party the power to direct and control the day-to-day activities of the other; (ii) constitute the parties as partners, joint ventures, co-owners or otherwise as participants in a joint or common undertaking; or (iii) allow Distributor to create or assume any obligation on behalf of Lazuriton Nano Biotech. All financial obligations associated with Distributor's business and its performance under this Agreement are the sole responsibility of Distributor. (h) Subdistributors. Distributor shall not appoint or use any third parties to market, sell or distribute the Products, unless such subdistributors, and Distributor's written agreement authorizing such subdistributor to market, sell or distribute Products, has been expressly approved by Lazuriton Nano Biotech in writing.
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Scope of the Agreement. Subject to the terms and conditions of this Agreement, Lazuriton Nano Biotech Shinin hereby appoints Distributor as an the authorized distributor of the Nano fertilizers Shinin products manufactured by Lazuriton Nano Biotech (the "Products") listed in Exhibit A (the "Products") A, and in the territory set forth on Exhibit A A, (the "Territory"), "Territory") and Distributor accepts such appointment. Distributor may not sell the Products to customers in another territory where Lazuriton Nano Biot...ech Shinin has reserved such territory exclusively for itself or another distributor. Distributor not, shall be prevented from directly or indirectly (including through its affiliates), actively solicit soliciting orders for any of the Products in any such that other territory; provided, however, Distributor shall not be prevented from accepting and filling unsolicited orders for the Products from a customer located outside the Territory. (b) Products. Lazuriton Nano Biotech Shinin reserves the right to discontinue or modify the Products, modify the Product specifications, or replace the Products with other Nano fertilizers Shinin products, in its sole discretion; provided, however, except as required by law, any such discontinuations, modifications, or replacements will not apply to Products that are subject to an outstanding purchase order accepted by Lazuriton Nano Biotech. Shinin. (c) Competitive Products. During the Term (as defined below), Distributor shall not promote or sell, directly or indirectly, any product manufactured or offered for sale by another person or entity, which product competes with the Products (each, a "Competing Product"). Distributor warrants that it does not promote or sell, directly or indirectly, any Competing Product as of the Effective Date. During the Term, Distributor shall disclose to Lazuriton Nano Biotech Shinin any new Nano fertilizers clothing products that Distributor intends to promote or sell, as well as the manufacturer of such products, prior to promoting or selling such products, and Lazuriton Nano Biotech Shinin shall determine, in its sole discretion, whether such products are Competing Products. (d) Independent Contractors. The relationship of Lazuriton Nano Biotech Shinin and Distributor established by this Agreement is that of independent contractors and nothing contained herein shall be construed to (i) give either party the power to direct and control the day-to-day activities of the other; (ii) constitute the parties as partners, joint ventures, co-owners co- owners or otherwise as participants in a joint or common undertaking; or (iii) allow Distributor to create or assume any obligation on behalf of Lazuriton Nano Biotech. Shinin. All financial obligations associated with Distributor's business and its performance under this Agreement are the sole responsibility of Distributor. (h) Subdistributors. Distributor shall not appoint or use any third parties to market, sell or distribute the Products, unless such subdistributors, and Distributor's written agreement authorizing such subdistributor to market, sell or distribute Products, has been expressly approved by Lazuriton Nano Biotech Shinin in writing.
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HAHA GENERATION CORP. contract